Paper Citing NAMD - Abstract
Grasso, Giuseppe; Pietropaolo, Adriana; Spoto, Giuseppe; Pappalardo, Giuseppe; Tundo, Grazia Raffaella; Ciaccio, Chiara; Coletta, Massimo; Rizzarelli, Enrico
Copper(I) and Copper(II) Inhibit A beta Peptides Proteolysis by Insulin-Degrading Enzyme Differently: Implications for Metallostasis Alteration in Alzheimer's Disease
CHEMISTRY-A EUROPEAN JOURNAL, 17:2752-2762, FEB 2011
Accumulation of neurotoxic amyloid-beta peptide (A beta) and alteration of metal homeostasis (metallostasis) in the brain are two main factors that have been very often associated with neurodegenerative diseases, such as Alzheimer's disease (AD). A beta is constantly produced from the amyloid-precursor-protein APP precursor and immediately catabolized under normal conditions, whereas dysmetabolism of A beta and/or metal ions seems to lead to a pathological deposition. Although insulin-degrading enzyme (IDE) is the main metalloprotease involved in A beta degradation in the brain being up-regulated in some areas of AD brains, the role of IDE for the onset and development of AD is far from being under-stood. Moreover, the biomolecular mechanisms involved in the recognition and interaction between IDE and its substrates are still obscure. In spite of the important role of metals (such as copper, aluminum, and zinc), which has brought us to propose a "metal hypothesis of AD", a targeted study of the effect of metallostasis on IDE activity has never been carried out. In this work, we have investigated the role that various metal ions (i.e., Cu2+, Cu+, Zn2+, Ag+, and Al3+) play in modulating the interaction between IDE and two A beta peptide fragments, namely A beta(1-16) and A beta(16-28). It was therefore possible to identify the direct effect that such metal ions have on IDE structure and enzymatic activity without interferences caused by metal-induced substrate modifications. Mass spectrometry and kinetic studies revealed that, among all the metal ions tested, only Cu2+, Cu+, and Ag+ have an inhibitory effect on IDE activity. Moreover, the inhibition of copper(II) is reversed by adding zinc(II), whereas the monovalent cations affect the enzyme activity irreversibly. The molecular basis of their action on the enzyme is also discussed on the basis of computational investigations.
